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   Congenital Adrenal Hyperplasia and Schmid Metaphyseal Chondrodysplasia in a Child  
   
نویسنده Khorasani Efat ,Vakili Rahim
منبع iranian journal of medical sciences - 2016 - دوره : 41 - شماره : 1 - صفحه:64 -66
چکیده    Congenital adrenal hyperplasia (cah) is a group of hereditary diseases, which are autosomal recessive. cah occurs due to defect in one of the cortisol coding genes and often clinically presents itself with signs of androgen overproduction. in this article, we report a case of cah and schmid metaphyseal dysplasia. our literature review indicated that this report is the first attempt on cyp11b1 and schmid dysplasia in a child.the specific diagnosis of 11-β-hydroxylase deficiency can be determined using high basal levels of deoxycorticosterone and/or 11-deoxycortisol serums.
کلیدواژه Adrenal hyperplasia . Congenital . Osteochondrodysplasias . Humans . Male
آدرس mashhad university of medical sciences, Imam Reza Hospital, Department of Pediatric Endocrinology, ایران, mashhad university of medical sciences, Imam Reza Hospital, Department of Pediatric Endocrinology, ایران
 
     
   
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